HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264307Generated: October 30, 2026
Hydrazinium chloride → HCID 178451527, compound
https://huagongshe.com/reaction/2264307
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrazinium chloride | HCID 115031 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | tert-Butyl 3-cyano-4-oxopyrrolidine-1-carboxylate | HCID 2756790 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178451527 | HCID 178451527 | — |
Reaction Steps
To a stirred solution of 1 g (4.76 mmol) of tert-butyl 3-cyano-4-oxopyrrolidine-1 carboxylate in ethanol (28 mL) was added 0.326 g (4.76 mmol) of hydrazine hydrochloride and the reaction mixture heated at ° C. for 3 h. The mixture was cooled to 0° C. and saturated aqueous sodium hydrogen carbonate (60 mL) added. The solvent was evaporated in vacuo and the aqueous phase extracted with ethyl acetate (10×10 mL). The combined organic fractions were dried (anhydrous sodium sulfate), filtered and the solvent evaporated in vacuo. The resulting residue was chromatographed on a Biotage Horizon® system (silica gel, 0 to 10% methanol/ethyl acetate gradient) to yield the title compound as a orange solid. LC/MS 225.2 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07855206B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-e84d2257fb244c1580ba909c5185f7e4 |
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| Source note | uspto-grants-2010_12 |
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